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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2013 2
2016 4
2017 2
2018 3
2019 3
2020 4
2021 2
2024 0

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18 results

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Page 1
Peculiar footprints in a child with agenesis of corpus callosum.
Cappuccio G, Genesio R, Pignataro P, Brunetti-Pierri N. Cappuccio G, et al. Among authors: pignataro p. J Paediatr Child Health. 2021 Mar;57(3):450-451. doi: 10.1111/jpc.1_15176. J Paediatr Child Health. 2021. PMID: 33728780 No abstract available.
A small 7q11.23 microduplication involving GTF2I in a family with intellectual disability.
Pinelli M, Terrone G, Troglio F, Squeo GM, Cappuccio G, Imperati F, Pignataro P, Genesio R, Nitch L, Del Giudice E, Merla G, Testa G, Brunetti-Pierri N. Pinelli M, et al. Among authors: pignataro p. Clin Genet. 2020 Jun;97(6):940-942. doi: 10.1111/cge.13753. Epub 2020 Apr 29. Clin Genet. 2020. PMID: 32349160 Free PMC article.
The Pro12Ala polymorphism of PPARγ2 modulates beta cell function and failure to oral glucose-lowering drugs in patients with type 2 diabetes.
Masulli M, Della Pepa G, Cocozza S, Capasso M, Pignataro P, Vitale M, Gastaldelli A, Russo M, Dolce P, Riccardi G, Rivellese AA, Vaccaro O. Masulli M, et al. Among authors: pignataro p. Diabetes Metab Res Rev. 2021 Mar;37(3):e3392. doi: 10.1002/dmrr.3392. Epub 2020 Sep 2. Diabetes Metab Res Rev. 2021. PMID: 32783395
Two cases of 16q12.1q21 deletions and refinement of the critical region.
Apuzzo D, Cappuccio G, Vaisanen T, Alagia M, Pignataro P, Genesio R, Brunetti-Pierri N. Apuzzo D, et al. Among authors: pignataro p. Eur J Med Genet. 2020 Jun;63(6):103878. doi: 10.1016/j.ejmg.2020.103878. Epub 2020 Feb 8. Eur J Med Genet. 2020. PMID: 32045705
18 results